replacement available Recalls

1,215 recalls tagged with “replacement available”.

Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Syringe Recall for 1.75 Million Kits Over Adaptor Unwinding Risk (2026)

Medline Industries, LP recalls 1,752,096 NAMIC Angiographic Syringe kits worldwide, including the US and Canada. The recall stems from a post-market signal about the rotating adaptor unwinding during use. This may cause a loose connection or disconnection between the syringe and manifold. Health care providers and patients should stop using the devices and follow recall instructions.

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Syringe Recalled Globally Over Rotation Adaptor Risk (2026)

Medline Industries, LP recalled 149,439 NAMIC Angiographic Syringes worldwide, including the US and several international markets. The post-market signal shows a potential rotation adaptor unwinding during use, which can cause a loose or complete disconnect with the manifold. Health care providers and patients should stop using the devices and follow Medline's recall instructions.

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Syringes Recalled Globally for Rotating Adaptor Unwinding Risk (Class I)

Medline Industries recalled 2,630,369 NAMIC Angiographic Syringes worldwide after post-market surveillance found a potential risk that the syringe rotating adaptor could unwind during use, causing a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions. Contact Medline or a healthcare provider for guidance.

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medical Convenience Kits Recalled Worldwide Over Rotating Adaptor Unwinding

Medline Industries, LP recalls 20 kits worldwide after post-market surveillance found a risk the syringe rotating adaptor may unwind during use, causing a loose connection or full disconnection with the manifold. The recall affects three Medline SKUs and includes UDI details and lot numbers. Healthcare providers and patients should stop using the device immediately and follow Medline's recall plan

Medline Industries, LP
Medline Industries,
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Health & Personal Care
HIGH
FDA DRUG

Macleods Pharma USA Recalls 1,315 Levothyroxine 150 mcg Tablets (2026)

Macleods Pharma USA, Inc. recalls 1,315 bottles of Levothyroxine Sodium Tablets USP 150 mcg distributed nationwide. The drug is subpotent, which may not provide the full therapeutic dose. Stop using and contact your healthcare provider or Macleods Pharma USA, Inc. for guidance.

LEVOTHYROXINE SODIUM
Subpotent Drug
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Recalls 370 kg Pepsin 1:10,000 Powder Over Salmonella Risk (2026)

American Laboratories recalled 370 kg of Pepsin 1:10,000 Powder sold through 11 wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one account in Australia after a potential Salmonella contamination. The product carries a possible Salmonella contamination risk. Consumers should not consume the product and should contact American Laboratories for refund or replacement via email.

American Laboratories
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Pepsin Full Strength Powder Recalled for Salmonella Contamination (400 kg, 202

American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,

American Laboratories
Potential Salmonella
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Health & Personal Care
HIGH
FDA DEVICE

Synthes Bone Taps Recall 33-Unit Lot Swap Causes Incorrect Threading (2026)

Synthes bone taps recalled nationwide in the United States after a lot swap affected 33 units sold through multiple retailers. The defect is an incorrect thread caused by a lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8. Healthcare providers should stop using these devices immediately and follow recall instructions from Synthes.

Synthes
A full
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recall: 93 PKS Cutting Forceps Over Welding Defects (2026)

Olympus Corporation of the Americas recalled 93 PKS Cutting Forceps worldwide due to welding defects that can cause the jaw to break during clinical use. The issue involves Model 3005PK and UDI 00821925036000. Action is required immediately and providers should follow recall instructions.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Everest Bipolar Cutting Forceps 3005 Recalled for Jaw Break Risk in 2026

Olympus Corporation of the Americas is recalling 106 Everest Bipolar Cutting Forceps worldwide. The devices can have welding defects that may cause the jaw to break during use. Stop using immediately and contact Olympus or your healthcare provider for instructions.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus HALO PKS Cutting Forceps HACF0533 Recalled for Jaw Breakage; 2,648 Units Worldwide (2026)

Olympus Corporation of the Americas is recalling 2,648 HALO PKS Cutting Forceps HACF0533 sold to hospitals and clinics worldwide. The jaw can break during surgical use due to a supplier welding-validation issue. Healthcare facilities should stop using the device immediately and follow Olympus recall instructions for disposition.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus PKS Cutting Forceps 920005PK Recalled for Jaw Break Risk (2026)

Olympus Corporation of the Americas recalled 326 PKS Cutting Forceps worldwide. The devices may have welding defects that cause the jaw to break during use. Stop using the device immediately and follow the recall instructions provided by Olympus.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus PK Cutting Forceps Recall 444 Units Worldwide Over Welding Defect (2026)

Olympus Corporation of the Americas is recalling 444 PK-CF0533 cutting forceps distributed worldwide. The devices may have welding defects that can cause the jaw to break during surgery. Stop using the device and follow recall instructions from Olympus or your healthcare provider.

Olympus Corporation of the Americas
Olympus identified
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Food & Beverages
HIGH
FDA FOOD

Novamex Coconut Water Recall Targets 12,000 Cases Over Packaging Nutrition Facts Discrepancy

A Tipp Distributors, Inc. dba Novamex recall affects 12,000 cases of C2O Coconut Water with Pulp sold across multiple states. The outer cardboard box lists an incorrect Nutrition Facts Panel and Ingredient List, omitting added sugar. The can itself has the correct information. Consumers should avoid consumption and seek refund or replacement.

Novamex
The outer
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Food & Beverages
HIGH
FDA FOOD

King Harvest Balsamic Hummus Recalled for Aluminum Shards in 326 10oz Tubs (2026)

King Harvest Balsamic Hummus recalled by Pacific Coast Fresh Co. The product was distributed in Oregon and Washington. A foreign material aluminum piece hazard was identified. Consumers should not eat the product and should contact Pacific Coast Fresh Co for refund or replacement information by telephone.

Pacific Coast Fresh CO
Foreign material
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Food & Beverages
HIGH
FDA FOOD

Pacific Coast Fresh CO Recalls King Harvest Sundried Tomato Hummus Over Aluminum Pieces (2026)

Pacific Coast Fresh CO recalls 348 10-ounce King Harvest Sundried Tomato Hummus containers sold in Oregon and Washington after aluminum pieces were found. The hazard is foreign material aluminum pieces in the hummus. Consumers should not consume the product and should contact Pacific Coast Fresh CO by telephone for refund or replacement.

Pacific Coast Fresh CO
Foreign material
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Food & Beverages
HIGH
FDA FOOD

Pacific Coast Fresh CO Recalls King Harvest Spinach Hummus 2026 for Aluminum Fragments

Pacific Coast Fresh CO is recalling 239 containers of King Harvest Spinach Hummus sold in Oregon and Washington. Each 10-ounce tub bears UPC 025726311087 and Best By date 2/27/2026. Stop using the product immediately due to aluminum fragments and call Pacific Coast Fresh CO by telephone for refund or replacement.

Pacific Coast Fresh CO
Foreign material
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Tag Statistics

Total Recalls
1,215

Related Tags

fire hazardelectrical hazardchemical hazardinfant producttoddler productadult productelderly productimmediate actionstop use immediatelyreturn for refundfederal law violationcpsc regulated